List of variants in gene ABCD1 reported as likely benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000033.4(ABCD1):c.757C>G (p.Leu253Val)	rs150151955	0.00060
NM_000033.4(ABCD1):c.50G>A (p.Arg17His)	rs782693577	0.00011
NM_000033.4(ABCD1):c.55G>T (p.Ala19Ser)	rs965462099	0.00005
NM_000033.4(ABCD1):c.1865+11C>T	rs781956636	0.00004
NM_000033.4(ABCD1):c.2173G>A (p.Ala725Thr)	rs782809184	0.00004
NM_000033.4(ABCD1):c.-20C>T	rs782004770
NM_000033.4(ABCD1):c.144G>A (p.Ala48=)	rs1557052209
NM_000033.4(ABCD1):c.1634+13G>A
NM_000033.4(ABCD1):c.1748T>A (p.Val583Glu)	rs79383557
NM_000033.4(ABCD1):c.1816T>C (p.Ser606Pro)	rs201774661

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